Department of Biology, Providence College, Providence, Rhode Island, United States of America.
PLoS One. 2013 May 15;8(5):e63982. doi: 10.1371/journal.pone.0063982. Print 2013.
Past studies have shown that birds use their wings not only for flight, but also when ascending steep inclines. Uphill flap-running or wing-assisted incline running (WAIR) is used by both flight-incapable fledglings and flight-capable adults to retreat to an elevated refuge. Despite the broadly varying direction of travel during WAIR, level, and descending flight, recent studies have found that the basic wing path remains relatively invariant with reference to gravity. If so, joints undergo disparate motions to maintain a consistent wing path during those specific flapping modes. The underlying skeletal motions, however, are masked by feathers and skin. To improve our understanding of the form-functional relationship of the skeletal apparatus and joint morphology with a corresponding locomotor behavior, we used XROMM (X-ray Reconstruction of Moving Morphology) to quantify 3-D skeletal kinematics in chukars (Alectoris chukar) during WAIR (ascending with legs and wings) and ascending flight (AF, ascending with wings only) along comparable trajectories. Evidence here from the wing joints demonstrates that the glenohumeral joint controls the vast majority of wing movements. More distal joints are primarily involved in modifying wing shape. All bones are in relatively similar orientations at the top of upstroke during both behaviors, but then diverge through downstroke. Total excursion of the wing is much smaller during WAIR and the tip of the manus follows a more vertical path. The WAIR stroke appears "truncated" relative to ascending flight, primarily stemming from ca. 50% reduction in humeral depression. Additionally, the elbow and wrist exhibit reduced ranges of angular excursions during WAIR. The glenohumeral joint moves in a pattern congruent with being constrained by the acrocoracohumeral ligament. Finally, we found pronounced lateral bending of the furcula during the wingbeat cycle during ascending flight only, though the phasic pattern in chukars is opposite of that observed in starlings (Sturnus vulgaris).
过去的研究表明,鸟类不仅用翅膀飞行,还在攀登陡峭的斜坡时使用翅膀。无法飞行的雏鸟和有飞行能力的成鸟都使用上坡拍打跑或翼辅助爬坡跑(WAIR)来退回到高处的避难所。尽管在 WAIR、水平和下降飞行期间旅行方向广泛变化,但最近的研究发现,基本的翅膀路径相对于重力仍然相对不变。如果是这样,关节会进行不同的运动,以在这些特定的拍打模式中保持一致的翅膀路径。然而,基础骨骼运动被羽毛和皮肤所掩盖。为了提高我们对骨骼装置和关节形态与相应的运动行为的形式功能关系的理解,我们使用 XROMM(移动形态的 X 射线重建)来量化鹧鸪(Alectoris chukar)在 WAIR(腿部和翅膀上升)和上升飞行(AF,仅翅膀上升)期间 3-D 骨骼运动学,沿着类似的轨迹。这里来自翅膀关节的证据表明,盂肱关节控制了翅膀运动的绝大部分。更远端的关节主要参与改变翅膀形状。在两种行为中,翅膀在上升行程的顶部,所有骨头都处于相对相似的取向,但在下降行程中则发散。在 WAIR 期间,翅膀的总行程要小得多,并且 manus 的尖端遵循更垂直的路径。与上升飞行相比,WAIR 冲程似乎“截断”,主要是由于肱骨下降减少了约 50%。此外,在 WAIR 期间,肘部和手腕的角运动范围减小。盂肱关节的运动模式与被肩锁韧带约束一致。最后,我们发现只有在上升飞行期间,叉骨在翅膀拍打周期中会出现明显的侧向弯曲,尽管鹧鸪的相位模式与星椋鸟(Sturnus vulgaris)观察到的相反。